» Articles » PMID: 26771592

Antibacterial Activity and Antibiotic-Enhancing Effects of Honeybee Venom Against Methicillin-Resistant Staphylococcus Aureus

Overview
Journal Molecules
Publisher MDPI
Specialty Biology
Date 2016 Jan 16
PMID 26771592
Citations 16
Authors
Affiliations
Soon will be listed here.
Abstract

Methicillin-resistant Staphylococcus aureus (MRSA), along with other antibiotic resistant bacteria, has become a significant social and clinical problem. There is thus an urgent need to develop naturally bioactive compounds as alternatives to the few antibiotics that remain effective. Here we assessed the in vitro activities of bee venom (BV), alone or in combination with ampicillin, penicillin, gentamicin or vancomycin, on growth of MRSA strains. The antimicrobial activity of BV against MRSA strains was investigated using minimum inhibitory concentrations (MIC), minimum bactericidal concentrations (MBC) and a time-kill assay. Expression of atl which encodes murein hydrolase, a peptidoglycan-degrading enzyme involved in cell separation, was measured by reverse transcription-polymerase chain reaction. The MICs of BV were 0.085 µg/mL and 0.11 µg/mL against MRSA CCARM 3366 and MRSA CCARM 3708, respectively. The MBC of BV against MRSA 3366 was 0.106 µg/mL and that against MRSA 3708 was 0.14 µg/mL. The bactericidal activity of BV corresponded to a decrease of at least 3 log CFU/g cells. The combination of BV with ampicillin or penicillin yielded an inhibitory concentration index ranging from 0.631 to 1.002, indicating a partial and indifferent synergistic effect. Compared to ampicillin or penicillin, both MRSA strains were more susceptible to the combination of BV with gentamicin or vancomycin. The expression of atl gene was increased in MRSA 3366 treated with BV. These results suggest that BV exhibited antibacterial activity and antibiotic-enhancing effects against MRSA strains. The atl gene was increased in MRSA exposed to BV, suggesting that cell division was interrupted. BV warrants further investigation as a natural antimicrobial agent and synergist of antibiotic activity.

Citing Articles

Natural Sources of Therapeutic Agents Used in Skin Conditions.

Dinu M, Tatu A, Cocos D, Nwabudike L, Chirilov A, Stefan C Life (Basel). 2024; 14(4).

PMID: 38672762 PMC: 11051086. DOI: 10.3390/life14040492.


Bee chitosan nanoparticles loaded with apitoxin as a novel approach to eradication of common human bacterial, fungal pathogens and treating cancer.

Sharaf M, Zahra A, Alharbi M, Mekky A, Shehata A, Alkhudhayri A Front Microbiol. 2024; 15:1345478.

PMID: 38559346 PMC: 10978808. DOI: 10.3389/fmicb.2024.1345478.


Structure-function-guided design of synthetic peptides with anti-infective activity derived from wasp venom.

Boaro A, Ageitos L, Torres M, Blasco E, Oztekin S, de la Fuente-Nunez C Cell Rep Phys Sci. 2024; 4(7).

PMID: 38239869 PMC: 10795512. DOI: 10.1016/j.xcrp.2023.101459.


Chemical composition and antibacterial activity of bee venom against multi-drug resistant pathogens.

Gokmen T, Yazgan H, Ozdemir Y, Sevin S, Turut N, Karahan S Onderstepoort J Vet Res. 2023; 90(1):e1-e5.

PMID: 37526529 PMC: 10483431. DOI: 10.4102/ojvr.v90i1.2097.


Antimicrobial Activity of Bee Venom Collected in Northern Peru.

Perez-Delgado O, Espinoza-Culupu A, Lopez-Lopez E Antibiotics (Basel). 2023; 12(4).

PMID: 37107142 PMC: 10135115. DOI: 10.3390/antibiotics12040779.


References
1.
Climo M, Patron R, Archer G . Combinations of vancomycin and beta-lactams are synergistic against staphylococci with reduced susceptibilities to vancomycin. Antimicrob Agents Chemother. 1999; 43(7):1747-53. PMC: 89355. DOI: 10.1128/AAC.43.7.1747. View

2.
Odds F . Synergy, antagonism, and what the chequerboard puts between them. J Antimicrob Chemother. 2003; 52(1):1. DOI: 10.1093/jac/dkg301. View

3.
Castro H, Mendez-Lnocencio J, Omidvar B, Omidvar J, Santilli J, Nielsen Jr H . A phase I study of the safety of honeybee venom extract as a possible treatment for patients with progressive forms of multiple sclerosis. Allergy Asthma Proc. 2006; 26(6):470-6. View

4.
Son D, Lee J, Lee Y, Song H, Lee C, Hong J . Therapeutic application of anti-arthritis, pain-releasing, and anti-cancer effects of bee venom and its constituent compounds. Pharmacol Ther. 2007; 115(2):246-70. DOI: 10.1016/j.pharmthera.2007.04.004. View

5.
Shahverdi A, Fakhimi A, Zarrini G, Dehghan G, Iranshahi M . Galbanic acid from Ferula szowitsiana enhanced the antibacterial activity of penicillin G and cephalexin against Staphylococcus aureus. Biol Pharm Bull. 2007; 30(9):1805-7. DOI: 10.1248/bpb.30.1805. View